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All product recalls associated with Ethicon Endo-Surgery Inc.
Total Recalls
73
Past Year
2
Class I (Serious)
0
Most Recent
Sep 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Mislabeled: Labeled on the package as 60mm contains 45mm devices
Product distributed with a red tape as part of the sterile packaging which could impact the seal and result in a sterility breach
The firm is recalling the PROCEED Surgical Mesh device, because it is a sterile device, and a customer found a hair inside of the primary packaging of a single unit.